Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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This is a sap recall not web posted. insufficient taper torsional strength may result when a par extension piece is used with a forged cocr stem. stryker received two reports indicating rotation or disassociation of a par extension piece when used in combination with a forged cocr stem. in each case rotation or dissociation was reported to occur upon initial weight bearing post-surgery.